- Collect and manage safety data in clinical trials and post-approval
- Support safety data capture, management and reporting for drugs, biologics, devices and vaccine products
- Boost productivity of safety departments with automation
- Drive regulatory compliance with workflow management tools for timely reporting
- Submit adverse event reports electronically
- Reduce IT expense with webbased software for end users and administrators
- Leverage signal detection in the clinical development and post-approval phases of the product lifecycle
Key Features Include:
- Web-based, 2nd generation design
- Easy-to-use interface
- Workflow support for paper or electronic case processing
- Required regulatory reporting for the US, EMEA and Japan
- Dynamic reporting environment
- Comprehensive coding support
- Easily integrated with existing homegrown and third party systems
Website: https://www.phaseforward.com/
Product brochure: https://www.phaseforward.com/jp/products/safety/aer/documents/ClintraceDataSheet072506.pdf
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